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M Abuín

Publications and source records attributed to M Abuín.

7 recordsLinked to original sources
PubMed2002

Methylmercury determination in biological samples by derivatization, solid-phase microextraction and gas chromatography with microwave-induced plasma atomic emission spectrometry.

A method for the extraction and gas chromatographic determination of methylmercury in biological matrices is presented. By combining the advantages of two extraction techniques-microwave-assisted extraction (MAE) and solid-phase microextraction (SPME)--the separation of methylmercury from biological samples is possible. Specifically, the procedure involves microwave extraction with 3 M hydrochloric acid, followed by aqueous-phase derivatization with sodium tetraphenylborate and headspace SPME with a silica fibre coated with polydimethylsiloxane (PDMS). For optimization of the derivatization-SPME procedure, a central composite experimental design with alpha = 1.682 and two central points was used to model gas-chromatographic peak areas as functions of pH, extraction temperature and sorption time. A desirability function was then used for the simultaneous optimization for methylmercury and Hg(II). The optimal derivatization-SPME conditions identified were close to pH 5, temperature 100 degrees C, and sorption time 15 min. The identification and quantification of the extracted methylmercury is carried out by gas chromatography with microwave-induced plasma atomic emission spectrometry detection. The validity of the new procedure is shown by the results of analyses of certified reference materials.

Calibration↗
PubMed2000

Experimental design of a microwave-assisted extraction-derivatization method for the analysis of methylmercury.

A simultaneous microwave-assisted extraction-derivatization procedure was developed and optimized for methylmercury analysis from biological samples. The analyte was derivatized with sodium tetraphenylborate forming a more hydrophobic compound, methylphenylmercury, which was extractable in toluene. The microwave extraction-derivatization procedure was optimized using experimental design, 2(5-1) fractional factorial. This chemometrical approach considers main effects as well as interactions of the influential parameters, indicating that temperature and its interaction with NaBPh4 and acetic acid volumes were the variables that significantly affected methylmercury recoveries.

Calibration↗
PubMed1996

A NOR-associated repetitive element present in the genome of two Salmo species (Salmo salar and Salmo trutta).

A repetitive element was isolated from the genome of Atlantic salmon. Nucleotide sequence analysis revealed the existence of variant monomers that range in length from approximately 200 to 230 bp. Repeat monomers contain regions of cryptic simplicity, internal repetition, and long direct repeats with deletions and insertions between individual units. The repetitive element was shown to have a tandem unit arrangement and was estimated to occupy between two and three percent of the Atlantic salmon genome. Southern blot analysis revealed the repetitive element to be unique to Atlantic salmon and brown trout species. In situ hybridization analysis showed this element to be localized at the main nucleolar organizer region bearing chromosomes of Atlantic salmon (Salmo salar), AS cell line (derived from S. salar), and brown trout (Salmo trutta).

Animals↗
PubMed1996

Localization of the repetitive telomeric sequence (TTAGGG)n in four salmonid species.

We have analyzed the localization of the highly conserved telomeric sequence (TTAGGG)n in four salmonid species, two of the genus Salmo (Salmo trutta and Salmo salar) and two of the genus Oncorhynchus (Onchorhynchus mykiss and Onchorhynchus kisutch), by fluorescent in situ hybridization. As expected, the hybridization signal was mostly localized at the telomeres of all chromosomes in the four species. Two species evidenced special hybridization sites with the telomeric probe: (i) interstitial heterochromatic blocks in particular long chromosomes in S. salar; this observation supports tandem fusions as the karyotypic evolutionary mechanism leading to the formation of the long acrocentric and submetacentric chromosomes in the karyotype of S. salar; (ii) the whole NOR region in O mykiss; this observation suggests that the (TTAGGG)n sequence is scattered all along this chromosome region.

Animals↗
PubMed1995

Restriction endonuclease/nick translation procedure on fixed chromosomes of the Atlantic salmon fish cell line.

We have used a restriction endonuclease/nick translation (RE/NT) procedure to study the ability of restriction enzymes to cleave DNA in fixed chromosomes of a fish cell line. This technique has proved to be very useful in revealing the chromatin heterogeneity underlying the chromosome structure that remains cryptic to other techniques also able to induce longitudinal differentiation on fish chromosomes. The differences observed in the banding patterns after nick translation procedure seem to be due, at least in part, to differences in activity among the enzymes assayed. The results obtained also reveal some evidence about the origin and evolution of the marker chromosomes of the Atlantic salmon cell line.

Animals↗
PubMed1993

Cytogenetic characterization of the AS cell line derived from the Atlantic salmon (Salmo salar L.).

The chromosome complement of the fish cell line AS, derived from the Atlantic salmon (Salmo salar L., 2N = 58), was investigated by C-, Ag-NOR, restriction endonuclease, and BrdU-replication banding. The cell line has a modal chromosome number of 52 with a fixed number of chromosomal rearrangements. The variety of banding patterns obtained allowed us to identify three chromosome markers in the cell line. The identification of their possible origin and significance in karyotype evolution are discussed.

Animals↗